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松果菊苷是肉苁蓉的一种活性成分,通过抑制炎症过程和激活Akt/GSK3β信号通路,对海人酸诱导的大鼠模型发挥神经保护作用。

Echinacoside, an Active Constituent of Cistanche Herba, Exerts a Neuroprotective Effect in a Kainic Acid Rat Model by Inhibiting Inflammatory Processes and Activating the Akt/GSK3β Pathway.

作者信息

Lu Cheng Wei, Hsieh Hsi Lung, Lin Tzu Yu, Hsieh Ting Yang, Huang Shu Kuei, Wang Su Jane

机构信息

Department of Anesthesiology, Far-Eastern Memorial Hospital.

Department of Mechanical Engineering, Yuan Ze University.

出版信息

Biol Pharm Bull. 2018 Nov 1;41(11):1685-1693. doi: 10.1248/bpb.b18-00407. Epub 2018 Sep 8.

Abstract

Echinacoside is a major compound of Cistanche Herb and has glutamate release-inhibiting activity in the brain. Given the involvement of excitotoxicity caused by massive glutamate in the pathophysiology of epilepsy, we explored the antiepileptic effect of echinacoside on kainic acid-induced seizures in rats. The rats were intraperitoneally administrated echinacoside for 30 min prior to intraperitoneal injection with kainic acid. The results showed that kainic acid induced seizure-like behavioral patterns, increased glutamate concentrations, caused neuronal loss and microglial activation, and stimulated proinflammatory cytokine gene expression in the hippocampus. These kainic acid-induced alternations were found to be attenuated by echinacoside pretreatment. Furthermore, decreased Akt and glycogen synthase kinase 3β (GSK3β) phosphorylation as well as Bcl-2 expression in the hippocampus was reversed by the echinacoside pretreatment. These results demonstrate that echinacoside exert its antiepileptic and neuroprotective actions in a kainic acid rat model through suppressing inflammatory response and activating the Akt/GSK3β signaling. Therefore, the present study suggests that echinacoside is the potentially useful in the prevention of epilepsy.

摘要

紫锥菊苷是肉苁蓉的主要成分,在大脑中具有抑制谷氨酸释放的活性。鉴于大量谷氨酸引起的兴奋性毒性参与癫痫的病理生理过程,我们探讨了紫锥菊苷对大鼠海人酸诱导癫痫发作的抗癫痫作用。在腹腔注射海人酸前30分钟,给大鼠腹腔注射紫锥菊苷。结果显示,海人酸诱导了癫痫样行为模式,增加了谷氨酸浓度,导致神经元丢失和小胶质细胞活化,并刺激了海马中促炎细胞因子基因表达。发现这些海人酸诱导的改变被紫锥菊苷预处理减弱。此外,紫锥菊苷预处理逆转了海马中Akt和糖原合酶激酶3β(GSK3β)磷酸化以及Bcl-2表达的降低。这些结果表明,紫锥菊苷在海人酸大鼠模型中通过抑制炎症反应和激活Akt/GSK3β信号发挥其抗癫痫和神经保护作用。因此,本研究表明紫锥菊苷在预防癫痫方面可能有用。

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